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accession-icon GSE9735
B6_IL1218_WAP
  • organism-icon Mus musculus
  • sample-icon 9 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

Dataset of IL-12+IL-18 trated and Yersinia enterocolitica infected C57BL/6 NK cells

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE110346
Expression data from CTL and Tc17 cell
  • organism-icon Mus musculus
  • sample-icon 4 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

Goal of this study was to compare transcriptional changes in CTL cells compared to Tc17 cells

Publication Title

No associated publication

Sample Metadata Fields

Specimen part

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accession-icon GSE48536
Maize gene expression after infection of Ustilago maydis SG200 and SG200tin2
  • organism-icon Zea mays
  • sample-icon 9 Downloadable Samples
  • Technology Badge Icon Affymetrix Maize Genome Array (maize)

Description

Anthocyanin induction in plant is considered a general defense response against biotic and abiotic stresses. The infection by Ustilago maydis, the corn smut pathogen, is accompanied with anthocyanin induction in leaf tissue. We revealed that anthocyanin is intentionally induced by the virulence promoting secreted effector protein Tin2. Tin2 protein functions inside plant cells where it interacts with cytoplasmic maize protein kinase ZmTTK1. Tin2 masks an ubiquitin-proteasome degradation motif in ZmTTK1 leading to a more stable active kinase. Active ZmTTK1 controls transcriptional activation of genes in the anthocyanin biosynthesis pathway rerouting phenylalanine away from lignin biosynthesis.

Publication Title

A secreted Ustilago maydis effector promotes virulence by targeting anthocyanin biosynthesis in maize.

Sample Metadata Fields

Specimen part

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accession-icon SRP130256
RNAseq analysis of hematopoietic stem and progenitor cells of immunized and naive mice during Bordetella pertussis challenge
  • organism-icon Mus musculus
  • sample-icon 36 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 1500

Description

The goal was to characterize gene expression profiles of HSPCs in mice during Bordetella pertussis infection. Mice were immunized with acellular or whole cell pertussis vaccines. HSPCs were isolated by flow cytometric sorting and RNA was prepared for library prep and RNA seq analysis.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Age, Specimen part, Disease, Cell line, Treatment

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accession-icon SRP112747
Characterizing the innate and adaptive responses of immunized mice to Bordetella pertussis infection using in vivo imaging and transcriptomics analyses
  • organism-icon Mus musculus
  • sample-icon 32 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 1500

Description

Total transcriptome analysis of naive or vaccinated murine lungs, post-challenge with Bordatella pertussis. Mice were immunized with PBS, whole cell pertussis vaccine, acellular pertussis vaccine, and RTX (adenylate cyclase toxoid) vaccine. The mice were then infected with B. pertussis and at 1 or 6/9 days post-challenge total lung RNA was purified for RNA-seq analysis.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part, Disease, Cell line, Treatment

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accession-icon SRP158625
Sequencing of polysome-associated mRNA in VSV infected HeLa cells
  • organism-icon Homo sapiens
  • sample-icon 24 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Infection of mammalian cells with vesicular stomatitis virus (VSV) results in the inhibition of cellular gene expression. This host shut-off is achieved through viral mediated inhibition of cellular gene expression at multiple levels including transcription, mRNP nuclear-cytoplasmic export, and translation. To interrogate the effects of VSV infection on translation, we infected HeLa cells at MOI 10 for 2 or 6 hours and performed polysome profiling and deep sequenced total cytoplasmic mRNA as well as monosome- and polysome-associated mRNAs. Our data support a model where viral mRNA abundance contributes to host shut-off by dominating the pool of cytoplasmic mRNA.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part, Cell line, Treatment, Time

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accession-icon E-MEXP-1135
Transcription profiling of gastric tissues from mice infected with H. pylori strain SS1 for 6 or 12 months
  • organism-icon Mus musculus
  • sample-icon 14 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Expression 430A Array (moe430a)

Description

12 C57BL/6 mice were infected orogastrically with the H. pylori strain SS1. After 6 and 12 months, 3 non-infected and 3 infected mice were sacrificed and stomachs isolated. Gastric tissues were disaggregated and total RNA were isolated by TRIzol extraction and then purified on RNeasy minicolumns. After synthesis of the first cDNA strand (In vitrogen), the double-stranded cDNA was obtained and used to produce biotin-labeled cRNA (Enzo Diagnostic). FRagmented cRNA was hybridized to GeneChip Mouse expression array 430A (Affymetrix).

Publication Title

Interferon gamma-signature transcript profiling and IL-23 upregulation in response to Helicobacter pylori infection.

Sample Metadata Fields

Sex, Age, Specimen part, Disease, Subject, Time

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accession-icon E-MEXP-1305
Transcription profiling of wild type, DAL82 knock out, PDR3 knock out and UGA3 knock out yeast strains
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 14 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

Yeast knockout strains were constructed by the Yeast Deletion Project. Three biological replicates were analyzed for each strain. 5 ml cultures were inoculated at OD600 = 0.2 from saturated overnight cultures and grown to mid-log phase (OD600 = 0.6 - 0.8) in YPD media 37 or in phosphate-depleted media 38 at 30C. Cells were harvested by centrifugation and washed with nuclease-free water (Ambion). Total RNA was isolated immediately after harvest using the Ribopure Yeast RNA Isolation Kit (Ambion). 5 mg of total RNA was used to generate labeled probes with standard Affymetrix protocols.

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon E-MEXP-1183
Transcription profiling of wild type, lasR rhIR and rpoS Pseudomonas aeruginosa mutants treated with acyl-HSL to investigage quorum sensing during the logarithmic phase of growth
  • organism-icon Pseudomonas aeruginosa
  • sample-icon 10 Downloadable Samples
  • Technology Badge Icon Affymetrix Pseudomonas aeruginosa Array (paeg1a)

Description

Effect of acyl-HSL signal or ectopic lasR, rhlR, or rpoS expression on the advancement of quorum sensing gene expression during the logarithmic phase of growth

Publication Title

Early Activation of Quorum Sensing in Pseudomonas aeruginosa Reveals the Architecture of a Complex Regulon

Sample Metadata Fields

Compound

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accession-icon SRP188861
impact of TIFIA and UBF depletion on genome wide responses to dsDNA
  • organism-icon Homo sapiens
  • sample-icon 10 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Cells were transfected with control, TIF-IA, or UBF siRNAs prior to transfection of no DNA or dsDNA. The impact of TIF-IA depletion on gene expression and the impact of TIF-IA and UBF depletion on dsDNA-induced gene expression were assayed.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part, Cell line

View Samples
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refine.bio is a repository of uniformly processed and normalized, ready-to-use transcriptome data from publicly available sources. refine.bio is a project of the Childhood Cancer Data Lab (CCDL)

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Cite refine.bio

Casey S. Greene, Dongbo Hu, Richard W. W. Jones, Stephanie Liu, David S. Mejia, Rob Patro, Stephen R. Piccolo, Ariel Rodriguez Romero, Hirak Sarkar, Candace L. Savonen, Jaclyn N. Taroni, William E. Vauclain, Deepashree Venkatesh Prasad, Kurt G. Wheeler. refine.bio: a resource of uniformly processed publicly available gene expression datasets.
URL: https://www.refine.bio

Note that the contributor list is in alphabetical order as we prepare a manuscript for submission.

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